Non-Invasive Determination of Cardiac Output by Inertgas Rebreathing Method

NCT ID: NCT00479804

Last Updated: 2008-06-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

311 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-08-31

Study Completion Date

2007-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The cardiac output (CO) is an important parameter in the diagnosis and therapy of cardiac diseases. The current standard methods for the determination of the CO, however, are either invasive (e.g. right heart catheterization) or technically expendable and expensive (magnetic resonance tomography, MRT). The traditional non-invasive methods of determining the CO by rebreathing of carbon dioxide are easily carried out but suffer from methodical inaccuracies. Therefore the aim of the study at hand was to evaluate a new method for determining the CO by means of the inert gas rebreathing method.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cardiac Diseases

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

indication for CMR

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

inertgas rebreathing

determination of cardiac output by inertgas rebreathing

Intervention Type DEVICE

spirometry

spirometry for testing the ventilatory function

Intervention Type DEVICE

cardiac magnetic resonance imaging (CMR)

CMR examination which delivers the hemodynamic reference parameters

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Indication for CMR
* Ability of following instructions for rebreathing test
Minimum Eligible Age

14 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Universitätsmedizin Mannheim

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

University Hospital Mannheim

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Joachim Saur, Dr.

Role: STUDY_DIRECTOR

1st Department of Medicine

Jens Kaden, Dr.

Role: STUDY_CHAIR

1st Deparment of Medicine

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

1st Department of Medicine, University Hospital Mannheim

Mannheim, Baden-Wurttemberg, Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2006-067M-MA

Identifier Type: -

Identifier Source: org_study_id